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Cited 11 time in webofscience Cited 14 time in scopus
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A Colorimetric CO2 Hydration Assay for Facile, Accurate, and Precise Determination of Carbonic Anhydrase Activityopen access

Authors
Kim, Joo HyunJo, Byung Hoon
Issue Date
Nov-2022
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
enzyme assay; carbon dioxide hydration; carbonic anhydrase; Wilbur-Anderson
Citation
Catalysts, v.12, no.11
Indexed
SCIE
SCOPUS
Journal Title
Catalysts
Volume
12
Number
11
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/29803
DOI
10.3390/catal12111391
ISSN
2073-4344
Abstract
A simple, reliable, and universal method is demanded for routine determination of carbonic anhydrase (CA) activity, overcoming the limitations of previous assays that are inaccurate, complicated, expensive, or limited to a specific enzyme family. The most widely used Wilbur-Anderson assay was modified to improve the speed, accuracy, and precision by employing a temperature controllable UV/Vis spectrophotometer and the pH indicator phenol red. The experimental setting, measurement, and data analysis were facile and straightforward. The assay was validated using a commercially available bovine CA, showing that the obtained activity was directly proportional to the amount of enzyme. The measured activity (2540 WAU mg(-1)) agreed well with the previously reported data. The comparison results with esterase assay showed that the CO2 hydration assay should not be substituted by the esterase assay in the measurement of CA activity. The simple and reliable colorimetric method can be widely adopted for the routine determination of CO2 hydration activity, substituting for the traditional Wilbur-Anderson assay.
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